Volume 16 Supplement 1

Abstracts of the 17th Annual SCMR Scientific Sessions

Open Access

Synthetic phase sensitive inversion recovery late gadolinium enhancement from post-contrast T1-mapping shows excellent agreement with conventional PSIR-LGE for diagnosing myocardial scar

  • Goran Abdula1,
  • Peder Sörensson1,
  • Magnus Lundin1,
  • Jannike Svedin1,
  • Margareta Klein1,
  • Peter Kellman2,
  • Andreas Sigfridsson1 and
  • Martin Ugander1
Journal of Cardiovascular Magnetic Resonance201416(Suppl 1):P213


Published: 16 January 2014


Cardiac magnetic resonance (CMR) imaging using phase sensitive inversion recovery (PSIR) late gadolinium enhancement (LGE) is the in vivo reference standard for assessing focal myocardial scar. Post-contrast T1-mapping by Modified Look-Locker Inversion recovery (MOLLI) can be used to generate a Synthetic PSIR LGE (SynLGE) image with an image contrast similar to conventional LGE images. We aimed to identify focal myocardial scar by SynLGE and compare its diagnostic accuracy with the reference standard LGE. We hypothesized that SynLGE has an accuracy which approaches LGE for diagnosing focal myocardial scar.


Consecutive patients (n = 60, mean ± SD age 50 ± 17 years, 60% male) referred for clinical CMR at 1.5T (Siemens Avanto or Aera) received an intravenous contrast bolus (0.2 mmol/kg gadoteric acid, Gd-DOTA, Dotarem®). PSIR LGE (1.3 × 1.3 × 8 mm) and post-contrast MOLLI (1.4 × 1.4 × 6 mm, 5-3 acquisition scheme, motion corrected) were acquired starting 10-15 and 20-25 minutes post bolus, respectively. A cardiac short-axis stack and three long-axis views were acquired for SynLGE and LGE. SynLGE at TI 300 ms were generated off-line from post-contrast T1-maps, and an in-line version is now available. Only LGE and SynLGE images (no cine images) were analyzed by two blinded observers for agreement regarding localization and origin of myocardial scar on a per-patient basis. Identification of scar required confirmation in two contiguous or orthogonal slices.


Consensus identified scar by LGE in 17/60 (28%) patients. The interobserver disagreement prior to consensus was 11/60 (12%). Scar patterns were non-ischemic (n = 9), ischemic (n = 6) or both (n = 2). Compared to LGE, SynLGE yielded a diagnostic sensitivity of 17/23 (74%), specificity of 36/37 (97%), positive predictive value of 17/18 (94%), negative predictive value of 36/42 (86%), and an overall accuracy of 53/60 (88%). In cases where SynLGE missed a scar (n = 6), these were either small non-ischemic scars (n = 4) or infarction in a thin myocardial wall (n = 2). In one case, SynLGE identified a midmural non-ischemic scar not identified by LGE. See Figure 1.

Figure 1


Overall, SynLGE showed high agreement with LGE. There were fewer differences between consensus LGE and SynLGE than there were differences in interobserver comparison for LGE, suggesting clinical equivalence of LGE and SynLGE. Thus, conventional LGE may not be necessary when full left ventricular coverage post-contrast T1-maps with SynLGE are routinely acquired for myocardial extracellular volume assessment. SynLGE therefore has the potential to reduce total scan time, except in challenging cases where complementary LGE can be added.


Swedish Research Council, Swedish Heart and Lung Foundation, Stockholm County Council, Karolinska Institutet, Swedish Medical Assocation, Swedish Society of Medical Research, and The Kleberg, Osterman, Wiberg, Erling-Persson, and Grönberg Foundations.

Authors’ Affiliations

Karolinska Institutet


© Abdula et al.; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.